Doğanci Alper, Ataman Şebnem, Özdemirel Ali Erhan, Seçkin Recep Bülent, Yalçin Ayşe Peyman, Bavbek Sevim
Division of Rheumatology, Department of Physical Medicine and Rehabilitation, Faculty of Medicine, Sivas Cumhuriyet University, Sivas, Turkiye.
Division of Rheumatology, Department of Physical Medicine and Rehabilitation, Faculty of Medicine, Ankara University, Ankara, Turkiye.
Turk J Med Sci. 2024 May 16;54(6):1310-1318. doi: 10.55730/1300-0144.5914. eCollection 2024.
BACKGROUND/AIM: We aimed to investigate the relationship between serum antidrug antibodies (ADAbs), systemic hypersensitivity, or local injection site reactions to tumor necrosis factor (anti-TNF) drugs and to detect the role of skin tests in the diagnosis of hypersensitivity reactions (HSRs) against anti-TNFs.
Sixty-nine ankylosing spondylitis (AS) and 46 rheumatoid arthritis (RA) patients taking infliximab (IFX), adalimumab (ADA), and etanercept (ETN) were enrolled. The demographical data, erythrocyte sedimentation rate (ESR), and c-reactive protein (CRP) levels of the patients were determined, and the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) assessment for AS patients and DAS28 (disease activity score) for RA patients were assessed. Serum levels of anti-TNFs and ADAbs to these agents were measured with ELISA. These blood samples were taken 24 h before the next drug dose. The patients with anti-TNF-associated HSRs were evaluated with a skin-prick test (SPT) and intradermal test (IDT). Readings for the SPT and IDT were conducted after 15 min and 24, 48, and 72 h. Heel diameter of 3 mm or more greater than the negative control was considered positive for SPT, and if the size of the initial wheal had increased by at least 3 mm in diameter and was surrounded by erythema it was considered positive for IDT. Symptoms such as urticaria/angioedema and flushing were considered immediate-type HSRs. Findings developed at the injection site such as swelling and erythema were considered injection-site reactions (ISRs). An overall p < 0.05 was considered statistically significant.
A statistically significant association was found between HSRs (immediate type and ISRs) and IDT reported by patients taking biological drugs (p = 0.001). In the subgroup analysis, a statistically significant association was found between ISRs and IDT in those taking ADA and ETN (respectively p = 0.012, p = 0.013). No relationship was found between skin test positivity and the presence of IgG ADAbs to anti-TNFs or disease activity scores.
This study demonstrates that patients who exhibit ISRs to anti-TNFs produce notably positive results to IDT without maintaining a direct relationship to serum levels of ADAbs.
背景/目的:我们旨在研究血清抗药物抗体(ADAbs)、全身超敏反应或针对肿瘤坏死因子(抗TNF)药物的局部注射部位反应之间的关系,并检测皮肤试验在诊断抗TNF超敏反应(HSRs)中的作用。
纳入69例强直性脊柱炎(AS)患者和46例类风湿关节炎(RA)患者,这些患者正在使用英夫利昔单抗(IFX)、阿达木单抗(ADA)和依那西普(ETN)。测定患者的人口统计学数据、红细胞沉降率(ESR)和C反应蛋白(CRP)水平,并对AS患者进行巴斯强直性脊柱炎疾病活动指数(BASDAI)评估,对RA患者进行DAS28(疾病活动评分)评估。采用酶联免疫吸附测定法(ELISA)测量血清抗TNF水平和针对这些药物的ADAbs水平。这些血样在下一次给药前24小时采集。对抗TNF相关HSRs患者进行皮肤点刺试验(SPT)和皮内试验(IDT)评估。SPT和IDT分别在15分钟以及24、48和72小时后读取结果。SPT结果以足跟直径比阴性对照大3mm或更多为阳性,IDT结果以初始风团直径至少增加3mm且周围有红斑为阳性。荨麻疹/血管性水肿和潮红等症状被视为速发型HSRs。注射部位出现的肿胀和红斑等表现被视为注射部位反应(ISRs)。总体p<0.05被认为具有统计学意义。
在使用生物药物的患者中,HSRs(速发型和ISRs)与IDT之间存在统计学显著关联(p=0.001)。在亚组分析中,使用ADA和ETN的患者中,ISRs与IDT之间存在统计学显著关联(分别为p=0.012,p=0.013)。未发现皮肤试验阳性与抗TNF的IgG ADAbs存在或疾病活动评分之间存在关联。
本研究表明,对抗TNF出现ISRs的患者IDT结果显著为阳性,且与ADAbs血清水平无直接关系。